Mast Syndrome (MASTS)

Alias:

Spg21

Autosomal Recessive Spastic Paraplegia Type 21

Spastic Paraplegia 21, Autosomal Recessive

Autosomal Recessive Spastic Paraplegia 21

Hereditary Spastic Paraplegia 21

Masts

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Mast Syndrome, also known as spg21, is related to spastic paraplegia 34, x-linked and spastic paraplegia 14, autosomal recessive, and has symptoms including abnormal pyramidal signs An important gene associated with Mast Syndrome is SPG21 (SPG21 Abhydrolase Domain Containing, Maspardin). Affiliated tissues include brain and cerebellum, and related phenotypes are abnormal pyramidal sign and difficulty walking

Related ID：

MALACARDS：MST006

OMIM：248900

MESH：C565409